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(5E)-3-(4-methoxyphenyl)-5-(4-nitrobenzylidene)-2-phenyl-3,5-dihydro-4H-imidazol-4-one is a complex organic compound with a molecular formula of C23H18N3O5. It features a 4H-imidazol-4-one core structure, which is a type of imidazole derivative. The compound has a 5-(4-nitrobenzylidene) group, indicating the presence of a nitrobenzene moiety attached to the imidazole ring through a double bond. Additionally, it contains a 3-(4-methoxyphenyl) group, which is a methoxyphenyl group attached to the imidazole ring. The compound's structure is characterized by a 3,5-dihydro pattern, suggesting the presence of two hydrogen atoms in the 3 and 5 positions of the imidazole ring. This chemical is likely to be found in research settings, particularly in the fields of organic chemistry and medicinal chemistry, where it may be studied for its potential applications or properties.

6150-11-4

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6150-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6150-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6150-11:
(6*6)+(5*1)+(4*5)+(3*0)+(2*1)+(1*1)=64
64 % 10 = 4
So 6150-11-4 is a valid CAS Registry Number.

6150-11-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (5E)-3-(4-methoxyphenyl)-5-[(4-nitrophenyl)methylidene]-2-phenylimidazol-4-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:6150-11-4 SDS

6150-11-4Upstream product

6150-11-4Downstream Products

6150-11-4Relevant academic research and scientific papers

Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation

Devaraj, Subramanian,Jagdhane, Rajendra C.,Shashidhar, Mysore S.

experimental part, p. 1159 - 1166 (2009/10/04)

O-Alkylation of myo-inositol derivatives containing more than one hydroxyl group via their alkali metal alkoxides (sodium or lithium) preferentially occurs at a hydroxyl group having a vicinal cis-oxygen atom. In general the observed selectivity is relatively higher for lithium alkoxides than for the corresponding sodium alkoxide. The observed regioselectivity is also dependent on other factors such as the solvent and reaction temperature. A perusal of the results presented in this article as well as those available in the literature suggests that chelation of metal ions by inositol derivatives plays a significant role in the observed regioselectivity. Steric factors associated with the axial or equatorial disposition of the reacting hydroxyl groups do not contribute much to the outcome of these O-alkylation reactions. These results could serve as guidelines in planning synthetic strategies involving other carbohydrates and their derivatives.

Chelation-Assisted C-O Bond Cleavage of Ortho Esters. A Convenient Synthesis of myo-Inositol Derivatives Having Free Hydroxy Group(s) at Specific Position(s)

Yeh, Sue-Min,Lee, Gene Hsiang,Wang, Yu,Luh, Tien-Yau

, p. 8315 - 8318 (2007/10/03)

Reactions of ortho esters of myo-inositol 8 or 10 with 1-2 equiv of Grignard reagents in benzene-ether yield regio- and stereoselectively the corresponding ring opening products having a free hydroxy group at C-1. The regioselectivity is rationalized owing to the presence of the 2-methoxy group which will serve as an auxiliary to form a chelation complex 12 with magnesium. Inositol derivatives having two free hydroxy group at C-1 and C-3 positions can be achieved from reactions of 6 or 8 with excess Grignard reagents or under more drastic conditions. The reaction of 8b with excess LiAlH4/AlCl3, on the other hand, yields the corresponding 1,5-diol 19.

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